Anticoagulant pretreatment attenuates production of cytokine-induced neutrophil chemoattractant following ischemia-reperfusion of rat liver

被引:36
作者
Hisama, N
Yamaguchi, Y
Okajima, K
Uchiba, M
Murakami, K
Mori, K
Yamada, S
Ogawa, M
机构
[1] KUMAMOTO UNIV, SCH MED, DEPT SURG 2, KUMAMOTO 860, JAPAN
[2] KUMAMOTO UNIV, SCH MED, DEPT LAB MED, KUMAMOTO 860, JAPAN
[3] KUMAMOTO UNIV, SCH MED, DEPT MED, KUMAMOTO 860, JAPAN
[4] UNIV OCCUPAT & ENVIRONM HLTH, DEPT INTERNAL MED 1, KITAKYUSHU, FUKUOKA 807, JAPAN
关键词
cytokine-induced neutrophil chemoattractant; coagulation; ischemia-reperfusion injury; liver; rat;
D O I
10.1007/BF02088576
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
We investigated whether anticoagulation would diminish ischemia-reperfusion injury of the liver. Liver ischemia was induced in rats by occluding the portal vein for 30 min. Anticoagulant was injected intravenously 10 min before occlusion. Serum concentrations of cytokine-induced neutrophil chemoattractant (CINC) in untreated rats increased following reperfusion, reaching a peak at 6 hr, then decreasing gradually to control levels by 24 hr. CINC levels in rats pretreated with heparin (50 units/kg), AT-III (250 units/kg), or DEGR-Xa (10 mg/kg) peaked at 3 hr after reperfusion and declined to baseline within 12 hr; peak CINC values were significantly lower than in untreated control rats. Expression of CINC mRNA in liver tissue paralleled the CINC serum levels. Both myeloperoxidase activity and the number of neutrophils in the liver were decreased in the anticoagulant groups. In addition, significant correlations were observed between the maximum values of AST, ALT, and LDH versus the peak CINC levels following ischemia-reperfusion. These results indicate that the release of CINC after ischemia-reperfusion of the liver is mediated by activation of coagulation within the hepatic microcirculation.
引用
收藏
页码:1481 / 1486
页数:6
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